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FDA 510(k)

CODE-A-WELL SERIES 200 PLATE

K-Number: K841632 · 1984-05-25

ApplicantPlastic Injectors, Inc.
Decision Date1984-05-25
Product CodeLIB
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CODE-A-WELL SERIES 200 PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Plastic Injectors, Inc.. It received FDA 510(k) clearance on 1984-05-25 under 510(k) number K841632. The device is classified under product code LIB. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CODE-A-WELL SERIES 200 PLATE?

CODE-A-WELL SERIES 200 PLATE is a medical device that received FDA 510(k) clearance on 1984-05-25. The listed applicant is Plastic Injectors, Inc.. The 510(k) number is K841632.

When did CODE-A-WELL SERIES 200 PLATE receive FDA 510(k) clearance?

CODE-A-WELL SERIES 200 PLATE received FDA 510(k) clearance on 1984-05-25, under 510(k) number K841632.

Who is the listed applicant for CODE-A-WELL SERIES 200 PLATE?

The FDA 510(k) record lists Plastic Injectors, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CODE-A-WELL SERIES 200 PLATE?

The FDA product code for CODE-A-WELL SERIES 200 PLATE is LIB.

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Other records listing Plastic Injectors, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K884781OPTI-POINTK863423CODE-A-WELL SERIES 1-1000 AND SERIES 1-1100K863374CODE-A-WELL SERIES 1-600, 1-625K844058CODE-A-WALL SERIES 1-250 INOCULUM TRAYK842848CODE-A-WELL 350 MICROTITRATION STRIPSK841937CODE-A-WELL SERIES 300 PLATE

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Related Devices (Code: LIB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K023677OSMETECH MICROBIAL ANALYSER-BACTERIAL VAGINOSIS (OMA-BV)OsmetechK920416SUPPLEMENTARY REAGENTS FOR ENZYGNOST/TMBBehring Diagnostics, Inc.K912558GULL ELISAWAREGull Laboratories, Inc.K872273CORNING EASY WASH ELISA PLATESCorning Medical & ScientificK871559CELL LIFTERCorning Costar Corp.K864249NORMAL SALINE STERILEMds Laboratories, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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